Hydrated C60 fullerene enhances parthanatos and induces autophagy-related biomarkers in glioblastoma cell line
Yıl 2022,
Cilt: 11 Sayı: 4, 88 - 97, 28.12.2022
Aryan M. Faraj
,
Victor Nedzvetsky
,
Artem Tykhomyrov
,
Gıyasettin Baydaş
,
Abdullah Aslan
,
Can Ali Agca
Öz
Glioblastoma is one the most aggressive type of brain cancers, which is resistant to resistant chemo- and radio-therapy. Nanoparticles of C60 fullerene derivates develop anticancer activity in various models. In contrast to many chemotherapy agents, this fullerene absolutely nontoxic in wide range of concentrations with respect to normal cells. C60 fullerene is a promising candidate for many biomedical applications. Therefore, we investigated the effect of water soluble hydrated C60 fullerene (HyC60Fn) on the expression of PARP, Beclin1, LC3, and GFAP in human glioblastoma U373 cell. Cell viability and migration were detected by MTT and wound healing-scratch assay, respectively. The expression of PARP, Beclin1, and LC3 were analyzed by western blotting and GFAP was detected with immunocytochemistry. HyC60Fn in a range of doses 0.5 – 2.0 µM decreased cell viability in a dose-dependent manner. Furthermore, the doses of HyC60Fn 1.0 and 2.0 µM noticeably suppressed glioblastoma cell migration. Mechanistically, we defined that HyC60Fn markedly up-regulated Beclin-1 and ratio of LC3-II/LC3-I expression as autophagy markers. Furthermore, water soluble HyC60Fn activated cleaved PARP fragment and consequently parthanatos in glioblastoma U373 cells. Present results demonstrate that HyC60Fn could initiate anti-tumor effect via the combination of severe autophagy flux and parthanatos in glioblastoma cells. Thus, HyC60Fn affects the cell death machinery, at least partially, through modulating glioblastoma cells reactivity and programmed cell death. Our findings suggest that pristine hydrated C60 fullerene could be a promising anti-cancer therapeutics and further study is required
Destekleyen Kurum
Scientific Research Projects Coordination Unit of Bingol University
Proje Numarası
BAP-5-317-2015 and BAP-FEF.2016.00.010.
Teşekkür
Scientific Research Projects Coordination Unit of Bingol University
Kaynakça
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Hydrated C60 fullerene, glioblastoma hücre hattında parthanatosu arttırır ve otofaji ile ilgili biyobelirteçleri indükler
Yıl 2022,
Cilt: 11 Sayı: 4, 88 - 97, 28.12.2022
Aryan M. Faraj
,
Victor Nedzvetsky
,
Artem Tykhomyrov
,
Gıyasettin Baydaş
,
Abdullah Aslan
,
Can Ali Agca
Öz
Glioblastoma, kemo ve radyoterapiye karşı dirençli, en agresif beyin kanseri tiplerinden biridir. C60 fulleren türevi nanopartiküller, çeşitli modellerde antikanser aktivite amacı ile geliştirilmektedir. Birçok kemoterapi ajanının aksine, bu fulleren çeşitli konsantrasyonlarda toksik değildir. C60 fulleren, birçok biyomedikal uygulama için umut verici bir adaydır. Bu nedenle, suda çözünür hydrated C60 fullerene'in (HyC60Fn) insan glioblastoma U373 hücresinde PARP, Beclin1, LC3 ve GFAP ekspresyonu üzerindeki etkileri araştırılmıştır. Hücre canlılığı ve göçü, sırasıyla MTT ve yara iyileşmesi testi ile belirlendi. PARP, Beclin1 ve LC3 ekspresyonu western blot ile ve GFAP ise immünositokimya ile tespit edildi. 0.5 – 2.0 µM doz aralığındaki HyC60Fn, doza bağlı bir şekilde hücre canlılığını azalttığı belirlendi. Ayrıca, HyC60Fn 1.0 ve 2.0 µM dozları, glioblastoma hücre göçünü belirgin şekilde bastırmıştır. Mekanizma olarak, HyC60Fn'nin otofaji belirteçleri olarak Beclin-1'i ve LC3-II/LC3-I ekspresyon oranını belirgin şekilde yukarı regüle ettiği belirlendi. Ayrıca, suda çözünür HyC60Fn’nin PARP fragmanı ve bu durumun doğal sonuç olarak glioblastoma U373 hücrelerinde parthanatos aktive ettiği belirlendi. Mevcut sonuçlar, HyC60Fn'nin, glioblastoma hücrelerinde şiddetli otofaji akışı ve parthanatos kombinasyonu yoluyla anti-tümör etkisini başlatabildiğini göstermektedir. Bu nedenle HyC60Fn, glioblastoma hücrelerinin reaktivitesini ve programlanmış hücre ölümünü modüle ederek en azından kısmen hücre ölüm mekanizmasını etkiler. Bulgularımız, HyC60Fn 'in umut verici bir kanser karşıtı terapötik olabileceğini ve bu konuda daha fazla çalışmanın gerekli olduğunu göstermektedir.
Proje Numarası
BAP-5-317-2015 and BAP-FEF.2016.00.010.
Kaynakça
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- 4. Song M, Yuan S, Yin J, Wang X, Meng Z, Wang H, et al. Size-dependent toxicity of nano-C60 aggregates: More sensitive indication by apoptosis-related bax translocation in cultured human cells. Environ Sci Technol [Internet]. 2012 Mar 20 [cited 2020 Jul 21];46(6):3457–64.
- 5. Hsieh FY, Zhilenkov A V., Voronov II, Khakina EA, Mischenko D V., Troshin PA, et al. Water-Soluble Fullerene Derivatives as Brain Medicine: Surface Chemistry Determines if They Are Neuroprotective and Antitumor. ACS Appl Mater Interfaces . 2017;9(13):11482–92.
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- 7. Jou MJ. Pathophysiological and pharmacological implications of mitochondria-targeted reactive oxygen species generation in astrocytes. Adv Drug Deliv Rev; 2008 p. 1512–26.
- 8. Larner SF, Wang J, Goodman J, O’Donoghue Altman MB, Xin M, Wang KKW. In vitro neurotoxicity resulting from exposure of cultured neural cells to several types of nanoparticles. Journal of Cell Death. Libertas Academica Ltd.; 2017
- 9. Biby TE, Prajitha N, Ashtami J, Sakthikumar D, Maekawa T, Mohanan P V. Toxicity of dextran stabilized fullerene C60 against C6 Glial cells. Brain Res Bull. 2020 Feb 1;155:191–201.
- 10. Johnston HJ, Hutchison GR, Christensen FM, Aschberger K, Stone V. The Biological Mechanisms and Physicochemical Characteristics Responsible for Driving Fullerene Toxicity. Toxicol Sci . 2010;9;114(2):162–82.
- 11. Trpkovic A, Todorovic-Markovic B, Trajkovic V. Toxicity of pristine versus functionalized fullerenes: Mechanisms of cell damage and the role of oxidative stress. Archives of Toxicology. Arch Toxicol; 2012 p. 1809–27.
- 12. Markovic Z, Trajkovic V. Biomedical potential of the reactive oxygen species generation and quenching by fullerenes (C60). Biomaterials. Biomaterials; 2008 p. 3561–73.
- 13. Li J, Tian M, Cui L, Dwyer J, Fullwood NJ, Shen H, et al. Low-dose carbon-based nanoparticle-induced effects in A549 lung cells determined by biospectroscopy are associated with increases in genomic methylation. Sci Rep. 2016 2;6(1):1–11.
- 14. Sosnowska M, Kutwin M, Jaworski S, Strojny B, Wierzbicki M, Szczepaniak J, et al. <p>Mechano-signalling, induced by fullerene C60 nanofilms, arrests the cell cycle in the G2/M phase and decreases proliferation of liver cancer cells</p>. Int J Nanomedicine. 2019, 6 14:6197–215.
- 15. Wierzbicki M, Sawosz E, Grodzik M, Prasek M, Jaworski S, Chwalibog A. Comparison of anti-angiogenic properties of pristine carbon nanoparticles. Nanoscale Res Lett. 2013;8(1):1–8.
- 16. Ye S, Chen M, Jiang Y, Chen M, Zhou T, Wang Y, et al. Polyhydroxylated fullerene attenuates oxidative stress-induced apoptosis via a fortifying Nrf2-regulated cellular antioxidant defence system. Int J Nanomedicine . 2014 29;9(1):2073–87.
- 17. Demir E, Nedzvetsky VS, Ağca CA, Kirici M. Pristine C60 Fullerene Nanoparticles Ameliorate Hyperglycemia-Induced Disturbances via Modulation of Apoptosis and Autophagy Flux. Neurochem Res. 2020;1;45(10):2385–97.
18. Kumari S, Badana AK, Murali Mohan G, Shailender G, Malla RR. Reactive Oxygen Species: A Key Constituent in Cancer Survival. Biomarker Insights. SAGE Publications Ltd; 2018.
- 19. Yang H, Villani RM, Wang H, Simpson MJ, Roberts MS, Tang M, et al. The role of cellular reactive oxygen species in cancer chemotherapy. Journal of Experimental and Clinical Cancer Research. BioMed Central Ltd.; 2018 p. 266.
- 20. Mijatović S, Savić-Radojević A, Plješa-Ercegovac M, Simić T, Nicoletti F, Maksimović-Ivanić D. The Double-Faced Role of Nitric Oxide and Reactive Oxygen Species in Solid Tumors. Antioxidants. 2020; 30;9(5):374.
- 21. Moloney JN, Cotter TG. ROS signalling in the biology of cancer. Seminars in Cell and Developmental Biology. Elsevier Ltd; 2018. p. 50–64.
- 22. Galadari S, Rahman A, Pallichankandy S, Thayyullathil F. Reactive oxygen species and cancer paradox: To promote or to suppress? Free Radical Biology and Medicine. Elsevier Inc.; 2017. p. 144–64.
- 23. Etem EO, Bal R, Akaǧaç AE, Kuloglu T, Tuzcu M, Andrievsky G V., et al. The effects of hydrated C(60) fullerene on gene expression profile of TRPM2 and TRPM7 in hyperhomocysteinemic mice. J Recept Signal Transduct. 2014;34(4):317–24.
- 24. Eisele G, Weller M. Targeting apoptosis pathways in glioblastoma [Internet]. Vol. 332, Cancer Letters. Elsevier Ireland Ltd; 2013. p. 335–45.
- 25. Wong RSY. Apoptosis in cancer: From pathogenesis to treatment [Internet]. Vol. 30, Journal of Experimental and Clinical Cancer Research. BioMed Central; 2011. p. 87.
- 26. Kaza N, Kohli L, Roth KA. Autophagy in brain tumors: A new target for therapeutic intervention. In: Brain Pathology. 2012. p. 89–98.
- 27. Yang K, Niu L, Bai Y, Le W. Glioblastoma: Targeting the autophagy in tumorigenesis. Vol. 153, Brain Research Bulletin. Elsevier Inc.; 2019. p. 334–40.
- 28. Levine B, Kroemer G. Autophagy in the Pathogenesis of Disease. Vol. 132, Cell. 2008. p. 27–42.
- 29. Feng F, Zhang M, Yang C, Heng X, Wu X. The dual roles of autophagy in gliomagenesis and clinical therapy strategies based on autophagic regulation mechanisms. Biomedicine and Pharmacotherapy. 2019.
- 30. Mizushima N, Levine B. Autophagy in mammalian development and differentiation. Vol. 12, Nature Cell Biology. Nature Publishing Group; 2010. p. 823–30.
- 31. Wang F, Jin C, Liang H, Tang Y, Zhang H, Yang Y. Effects of fullerene C60 nanoparticles on A549 cells. Environ Toxicol Pharmacol. 2014;1;37(2):656–61.
- 32. Hu Z, Guan W, Wang W, Zhu Z, Wang Y. Folacin C60 derivative exerts a protective activity against oxidative stress-induced apoptosis in rat pheochromocytoma cells. Bioorganic Med Chem Lett. 2010;15;20(14):4159–62.
- 33. Zhou YY, Li Y, Jiang WQ, Zhou LF. MAPK/JNK signalling: A potential autophagy regulation pathway. Biosci Rep. 2015;35(3):1–10.
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